SLC35B1 - solute carrier family 35 member B1 Gene

Also Known as AXER; UGTREL1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10237

About SLC35B1

Cytogenetic location: 17q21.33 Genomic coordinates (GRCh38): 17:49,700,943-49,708,197 (from NCBI)

This gene has 20 transcripts (splice variants), 203 orthologues and 3 paralogues. Ubiquitous expression in thyroid (RPKM 24.3), duodenum (RPKM 18.7) and 25 other tissues.

Summary

This gene encodes a nucleotide sugar transporter which is a member of solute carrier family 35. The transporters in this family are highly conserved hydrophobic proteins with multiple transmembrane domains. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]

SLC35B1 Products (2)

mRNA Protein Name
NM_001278784.2 NP_001265713.1 solute carrier family 35 member B1 isoform 2
NM_005827.4 NP_005818.3 solute carrier family 35 member B1 isoform 1
Molecular Function GO Annotation Evidence References Source
enables ATP:ADP antiporter activity IDA
IDA: Inferred from direct assay
30154480 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
Cellular Component GO Annotation Evidence References Source
located in endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
30154480 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC35B1 Protein Structure

UAA

UAA: UAA transporter family (16 - 315)

  • 0
  • 100
  • 200
  • 300
  • 322 a.a.
Protein Preferred Names Protein Names

solute carrier family 35 member B1

  • ATP/ADP exchanger ER

SLC35B1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SLC35B1 P78383 VAPA Homo sapiens Q9P0L0 32296183
Intra
SLC35B1 P78383 ARL13B Homo sapiens Q3SXY8 32296183
Intra
SLC35B1 P78383 ARL13B Homo sapiens Q3SXY8 32296183
Intra
SLC35B1 P78383 ARL13B Homo sapiens Q3SXY8 32296183
Intra
SLC35B1 P78383 MFF Homo sapiens Q9GZY8-5 32296183
Intra
SLC35B1 P78383 MFF Homo sapiens Q9GZY8-5 32296183
Intra
SLC35B1 P78383 MFF Homo sapiens Q9GZY8-5 32296183
Intra
SLC35B1 P78383 FXYD3 Homo sapiens Q14802-3 32296183
Intra
SLC35B1 P78383 FXYD3 Homo sapiens Q14802-3 32296183
Intra
SLC35B1 P78383 FXYD3 Homo sapiens Q14802-3 32296183
Intra
SLC35B1 P78383 PTPN5 Homo sapiens P54829 32296183
Intra
SLC35B1 P78383 PTPN5 Homo sapiens P54829 32296183
Intra
SLC35B1 P78383 CD74 Homo sapiens P04233-2 32296183
Intra
SLC35B1 P78383 CD74 Homo sapiens P04233-2 32296183
Intra
SLC35B1 P78383 AQP6 Homo sapiens Q13520 32296183
Intra
SLC35B1 P78383 AQP6 Homo sapiens Q13520 32296183
Intra
SLC35B1 P78383 AQP6 Homo sapiens Q13520 32296183
Intra
SLC35B1 P78383 GPR152 Homo sapiens Q8TDT2 32296183
Intra
SLC35B1 P78383 GPR152 Homo sapiens Q8TDT2 32296183
Intra
SLC35B1 P78383 GPR152 Homo sapiens Q8TDT2 32296183
Intra
SLC35B1 P78383 FZD5 Homo sapiens Q13467 32296183
Intra
SLC35B1 P78383 FZD5 Homo sapiens Q13467 32296183
Intra
SLC35B1 P78383 FZD5 Homo sapiens Q13467 32296183
Intra
SLC35B1 P78383 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
SLC35B1 P78383 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
SLC35B1 P78383 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
SLC35B1 P78383 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
SLC35B1 P78383 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
SLC35B1 P78383 PDZK1IP1 Homo sapiens Q13113 32296183
Intra
SLC35B1 P78383 FKBP8 Homo sapiens Q14318 32296183
Intra
SLC35B1 P78383 VSIR Homo sapiens Q9H7M9 32296183
Intra
SLC35B1 P78383 VSIR Homo sapiens Q9H7M9 32296183
Intra
SLC35B1 P78383 VSIR Homo sapiens Q9H7M9 32296183
Intra
SLC35B1 P78383 BNIP3 Homo sapiens Q12983 32296183
Intra
SLC35B1 P78383 CD79A Homo sapiens P11912 32296183
Intra
SLC35B1 P78383 CD79A Homo sapiens P11912 32296183
Intra
SLC35B1 P78383 CCDC107 Homo sapiens Q8WV48 32296183
Intra
SLC35B1 P78383 CCDC107 Homo sapiens Q8WV48 32296183
Intra
SLC35B1 P78383 CCDC107 Homo sapiens Q8WV48 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Barre-Lieou Syndrome
  • Cervicocranial Syndrome

  • Posterior Cervical Sympathetic Syndrome

Dicarboxylic Aminoaciduria
  • Glutamate-Aspartate Transport Defect

  • Dicarboxylicaminoaciduria

  • DCBXA

  • Renal Aminoacidurias

Bardet-Biedl Syndrome 10
  • BBS10

  • Bardet-Biedl Syndrome

  • Bbs

  • Bardet-Biedl Syndrome, Type 10

Hydranencephaly
  • Hydroanencephaly

Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb
  • Chromosome 1q21.1 Deletion Syndrome

  • 1q21.1 Microdeletion Syndrome

  • Monosomy 1q21.1

  • 1q21.1 Microdeletion

  • Chromosome 1q21.1 Microdeletion Syndrome

  • 1q21.1 Contiguous Gene Deletion

  • 1q21.1 Deletion

  • Del(1)(Q21)

  • 1q21.1 Deletion Syndrome

Retinitis Pigmentosa 12
  • RP12

  • Retinitis Pigmentosa With Or Without Paraarteriolar Preservation Of Retinal Pigment Epithelium

  • Rp With Or Without Preserved Paraarteriole Retinal Pigment Epithelium

  • Rp With Or Without Pprpe

  • Retinitis Pigmentosa-12

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus SLC35B1 MGD MGI:1343133
Rattus norvegicus SLC35B1 RGD RGD:727783
Macaca mulatta SLC35B1 VGNC VGNC:77533
Canis familiaris SLC35B1 VGNC VGNC:46364
Bos taurus SLC35B1 VGNC VGNC:34823
Felis catus SLC35B1 VGNC VGNC:65324
Others SLC35B1 NCBI